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Table 2 Single-marker analysis between SNPs and categorical DD.

From: Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children

rs Number SNP Position Location Allele F OR (95% CI) Nominal p-value FDR q-value
rs8040756 A/G 26589156 Intron 1 A* 0.135 1.43 (0.88 - 2.32) 0.1445 0.2823
     G 0.865    
rs3743205 G/A 26581087 5' UTR G* 0.982 0.08 (0.01 - 0.64) 0.0009 0.0072
     A 0.018    
rs4255730 C/T 26578338 Intron 3 C* 0.670 0.85 (0.59 - 1.23) 0.3969 0.6202
     T 0.330    
rs692646 A/G 26557344 Intron 4 A* 0.067 2.00 (0.96 - 4.12) 0.0532 0.1385
     G 0.933    
rs692691 C/T 26551132 Intron 4 C* 0.947 0.86 (0.40 - 1.85) 0.6947 0.8455
     T 0.053    
rs2290981 A/G 26550245 Intron 4 A* 0.119 1.10 (0.60 - 2.02) 0.7575 0.8455
     G 0.881    
rs4774768 G/T 26517062 Intron 8 G* 0.189 1.68 (1.02 - 2.76) 0.0367 0.1385
     T 0.811    
rs57809907 G/T 26513439 Exon 10 T* 0.004 1.00 (0.06 - 15.99) 1.0000 0.9766
     G 0.996    
  1. F = Allele frequency
  2. *Reference allele